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C33抗原(CD82)的小鼠同源物,跨膜4超家族成员:互补DNA、基因组结构及表达

Mouse homologue of C33 antigen (CD82), a member of the transmembrane 4 superfamily: complementary DNA, genomic structure, and expression.

作者信息

Nagira M, Imai T, Ishikawa I, Uwabe K I, Yoshie O

机构信息

Shionogi Institute for Medical Science, Osaka, Japan.

出版信息

Cell Immunol. 1994 Aug;157(1):144-57. doi: 10.1006/cimm.1994.1212.

Abstract

C33 Ag (CD82) is a member of the transmembrane 4 superfamily (TM4SF) and an activation Ag of T-cells. Recent studies have shown that CD82 associates with CD4 or CD8 and delivers costimulatory signals for the TCR/CD3 pathway. We have isolated cDNA and genomic clones of mouse CD82. Mouse CD82 has 266 amino acid residues with 76% identity to human CD82. The mouse CD82 gene consists of nine exons and spans more than 20 kb of genomic DNA. The genomic organization of CD82 is quite similar to that of three other TM4SF members whose genomic structures were described, i.e., Tapa-1 (CD81), CD53, and CD63. By mapping the 5' end of CD82 transcripts, we found a single major transcription initiation site 144 bp upstream of the ATG initiation codon. We also determined the sequence of the 5' flanking region of CD82 gene for about 2 kb. The 5' flanking sequence has a housekeeping promoter with potential binding motifs for various transcriptional factors. Northern blot analysis showed quite variable expression of the CD82 gene among different organs. The highest expression was seen in the spleen and the kidney. The expression was low in skeletal muscle and hardly detectable in the heart. Northern blot analysis was also carried out for CD81, CD53, and CD63. The expression of the CD81 gene was ubiquitous and similar among different organs, while that of CD53 was seen only in the spleen. The expression of the CD63 gene was ubiquitous, with the highest expression in the kidney. These results together with the comparison of the structures of 5' flanking sequences of these genes indicate distinct regulations of gene expression for these four members of TM4SF.

摘要

C33抗原(CD82)是跨膜4超家族(TM4SF)的成员之一,也是T细胞的激活抗原。最近的研究表明,CD82与CD4或CD8相关联,并为TCR/CD3途径传递共刺激信号。我们已经分离出小鼠CD82的cDNA和基因组克隆。小鼠CD82有266个氨基酸残基,与人CD82的同源性为76%。小鼠CD82基因由9个外显子组成,跨越超过20kb的基因组DNA。CD82的基因组结构与其他三个已描述基因组结构的TM4SF成员非常相似,即Tapa-1(CD81)、CD53和CD63。通过定位CD82转录本的5'末端,我们在ATG起始密码子上游144bp处发现了一个单一的主要转录起始位点。我们还确定了CD82基因5'侧翼区域约2kb的序列。5'侧翼序列有一个管家启动子,带有各种转录因子的潜在结合基序。Northern印迹分析显示,CD82基因在不同器官中的表达差异很大。在脾脏和肾脏中表达最高。在骨骼肌中表达较低,在心脏中几乎检测不到。我们也对CD81、CD53和CD63进行了Northern印迹分析。CD81基因的表达普遍存在,在不同器官中相似,而CD53仅在脾脏中表达。CD63基因的表达普遍存在,在肾脏中表达最高。这些结果以及这些基因5'侧翼序列结构的比较表明,TM4SF的这四个成员在基因表达调控上存在明显差异。

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